rs80357212(A;G)

BRCA1 variant of unclear significance

Is a	genotype
of	rs80357212
Gene	BRCA1
Chromosome	17
Position	43,047,643
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(A;G)	3	BRCA1 variant of unclear significance
(G;G)	0	common in clinvar

see discussion at rs80357212